- Healthcare Ethics
- Science and Research
- Good Clinical Practices (GCP)
- Clinical Research Ethics
- Clinical Trials
- Clinical Research
- Regulatory Compliance
- Biostatistics
- Informed Consent
Design and Conduct of Clinical Trials
Completed by Andjela Scekic
February 13, 2024
4 hours (approximately)
Andjela Scekic's account is verified. Coursera certifies their successful completion of Design and Conduct of Clinical Trials
What you will learn
Evaluate and select clinical trial designs
Implement bias control measures
Randomize participants into groups
Define clinical trial outcomes
Skills you will gain
